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Polymeric spinal fusion cage, non-sterile

Access comprehensive regulatory information for Polymeric spinal fusion cage, non-sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy Spine Inc in United States of America. The device registration started on April 01, 2019.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class IIb
Class IIb
Polymeric spinal fusion cage, non-sterile
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Polymeric spinal fusion cage, non-sterile
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Intended Purpose

A non-sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
April 01, 2019
Effective Date
April 01, 2019
Manufacturer
Country
United States of America
Address
325 Paramount Drive, Raynham, Massachusetts, 02767